investigation of electrical stimulation induced changes in nerves and muscles in individuals with post stroke paralysis
- Conditions
- Hemiplegia, unspecified,
- Registration Number
- CTRI/2024/02/062279
- Lead Sponsor
- PDUNIPPD
- Brief Summary
**the main purpose of our study is to examine the Functional Electrical Stimulation (FES) induced effects in the neuromuscular tissues (nerves and muscles); functional activities, muscle firing and spasticity in the post stroke hemiparetic individuals. The second purpose of our study is to correlate the FES induced effects in the neuromuscular tissues with the functional activities, muscle firing and spasticity in the upper extremity of post stroke hemiparetic individuals.**
**Alternate:**Functional Electrical Stimulation Produces Significant effects in Neuromuscular tissues and Functional Activities in post stroke hemiparetic individuals
**Null Hypothesis:** There is no significant effect of Functional Electrical Stimulation in
Neuromuscular tissues and Functional Activities in post stroke hemiparetic individuals
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 57
- Ipsilateral Hemiparesis following stroke either ischemic or hemorrhagic Three months to one year of the stroke.
- Hemiparesis having grade 1+ to 3 on Modified Ashworth Scale of Biceps Brachi, wrist flexors and finger flexors Individuals of the both the gender age group between 40 years and 60 years Both male and females Individual willing to participate voluntarily in the study.
- Bilateral Hemiparesis Hemiparesis following reason or caused other than stroke such as head injury, multiple sclerosis.
- Any previous history of stroke History of Brain or spinal cord tumor, injury or surgery Stroke patients having other co morbidities such as Alzemer,s disease, Parkinson’s disease, and dementia that preclude their participation in the study.
- Participants having severre spasticity and contracture in the elbow, hand and fingers.
- Individual with uncontrolled hypertension Individual with any systemic illness Individual with hypersensitivity or hypersensitivity disorders and Participants not able to follow the instructions and having difficulty in comprehension.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ELECTROMYOGRAPHY AND NERVE CONDUCTION VELOCITY STUDIES First outcome baseline assessment will be done at first visit before starting the intervention. | Second outcome assessment will be done at the end of fourth week of the study
- Secondary Outcome Measures
Name Time Method Fugal-Meyer Upper Extremity functional scale and modified Ashworth scale four weeks
Trial Locations
- Locations (1)
Pandit Deendayal Upadhyaya National Institute for the Persons with Physical Disabilities
🇮🇳Delhi, DELHI, India
Pandit Deendayal Upadhyaya National Institute for the Persons with Physical Disabilities🇮🇳Delhi, DELHI, IndiaROSHAN LAL MEENAPrincipal investigator9811368079roshan7leo@yahoo.com